| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42277159-42277284 | Rare:22 | ||||
| chr17:42288131-42288243 | Common:1; Rare:25 | ||||
| chr17:42288322-42288532 | Rare:40 | ||||
| chr17:42325119-42325264 | Rare:25 | ||||
| chr17:42388341-42388969 | Common:2; Rare:164; Clinvar:3 | ||||
| chr17:42389061-42389077 | Rare:6 | ||||
| chr17:42423151-42423514 | Common:1; Rare:95; Clinvar:1 | ||||
| chr17:42458673-42458948 | Common:3; Rare:102 | ||||
| chr17:42520102-42520390 | Common:1; Rare:61 | ||||
| chr17:42535920-42536358 | Common:4; Rare:121; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr17:42536397-42536475 | Rare:19; Clinvar:4 | ||||
| chr17:42536538-42536844 | Common:3; Rare:73; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr17:42536997-42537087 | Common:1; Rare:18 | ||||
| chr17:42561964-42562245 | Common:1; Rare:85 | ||||
| chr17:42562366-42562640 | Common:1; Rare:110; Clinvar:1; Clinvar (benign):2 |